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The presence of antibiotics in aquatic ecosystems poses a significant concern for public health and aquatic life, owing to their contribution to the proliferation of antibiotic-resistant bacteria. Effective wastewater treatment strategies are needed to ensure that discharges from pharmaceutical manufacturing facilities are adequately controlled. Here we propose the sequential use of nanofiltration (NF) for concentrating a real pharmaceutical effluent derived from azithromycin production, followed by electrochemical oxidation for thorough removal of pharmaceutical compounds. The NF membrane demonstrated its capability to concentrate wastewater at a high recovery value of 95 % and 99.7 ± 0.2 % rejection to azithromycin. The subsequent electrochemical oxidation process completely degraded azithromycin in the concentrate within 30 min and reduced total organic carbon by 95 % in 180 min. Such integrated treatment approach minimized the electrochemically-treated volume through a low-energy membrane approach and enhanced mass transfer towards the electrodes, therefore driving the process toward zero-liquid-discharge objectives. Overall, our integrated approach holds promises for cost-effective and sustainable removal of trace pharmaceutical compounds and other organics in pharmaceutical wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The ubiquitousness of per- and polyfluoroalkyl substances (PFAS) is a big concern and PFAS remediation is urgently needed such as via degradation. While previous studies have explored ultrasonic degradation of PFAS, work evaluating the operational parameters is rare, especially concerning real wastes such as aqueous film-forming foam (AFFF) and foam fractionate (FF). This study investigates the key operational parameters affecting the degradation efficiency of PFAS, encompassing ultrasonication frequency (580-1144 kHz), power intensity (125-187.5 W), initial concentration (0.08-40 ppm), treatment duration (0.5-3 h), sample volume (100-500 mL), and PFAS structure (perfluorooctanoic acid or PFOA; perfluorooctane sulfonate or PFOS; 6:2 fluorotelomer sulfonate or 6:2 FTS). The defluorination kinetics is different from the removal/degradation kinetics due to the generation of degradation intermediates, suggesting the complex degradation mechanism, which should be evaluated to close the mass balance effectively. Notably, the optimised ultrasonic system achieves ∼125%/∼115% defluorination in AFFF/FF example wastes (compared to ∼65%/∼97% removal) despite their complex composition and the involvement of total oxidizable precursor (TOP) assay. In the meantime, a few new PFAS are detected in the post-treatments, including perfluorohexane sulfonic acid (PFHxS) and 10:2 fluorotelomer sulfonate (10:2 FTS) in the AFFF, and perfluorooctane sulfonamide (FOSA) and 8:2 fluorotelomer sulfonate (8:2 FTS) in the FF, again suggesting the complex degradation mechanism. Overall, ultrasonication is effective to degrade PFAS real example wastes, advancing its potential for scale-up applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Perfluorooctanoic acid (PFOA) is an emerging persistent organic pollutant. Exposure to PFOA was observed to have a correlation with the expression levels of phospholipids. However, there are currently no studies that directly visualize the effects of PFOA on phospholipids. To this end, matrix-assisted laser desorption/ionization time of flight imaging mass spectrometry (MALDI-TOF-IMS) was used to visualize changes in phospholipids in the different tissues of zebrafish following exposure to PFOA. This study found that the major perturbed phospholipids were phosphatidylcholine (PC), diacylglycerol (DG), phosphatidic acid (PA), phosphatidylglycerol (PG), sphingomyelin (SM), and triacylglycerol (TG). These perturbed phospholipids caused by PFOA were reversible in some tissues (liver, gill, and brain) and irreversible in others (such as the highly exposed intestine). Moreover, the spatial distribution of perturbed phospholipids was mainly located around the edge or center of the tissues, implying that these tissue regions need special attention. This study provides novel insight into the biological toxicity and toxicity mechanisms induced by emerging environmental pollutants.

As an important class of disinfection byproducts (DBPs) of emerging concern, haloacetaldehydes (HALs) undergo degradation and transformation under environmentally relevant conditions. In this study, the stability of chlorinated and brominated HALs was investigated at different pHs and water temperatures. Results indicated that the degradation of HALs followed second-order kinetics. Surprisingly, rapid degradation of Br-HALs at elevated temperature was newly discovered in this study. At 50 °C and pH 7.5, over 90 % of TBAL degraded in 8 min, while the degradation of TCAL was ∼1 %. Moreover, increasing pH also facilitated the degradation of HALs and the alkaline degradation rate constants ( [Formula: see text] ) were found to be 7-9 orders of magnitude higher than their neutral degradation rate constants ( [Formula: see text] ). Under conditions relevant to environment and DBP measurement, HALs mainly degraded to form corresponding trihalomethanes and formate via decarburization pathway, which accounted for 70-93 % of HALs loss. The remaining 7-30 % of HAL loss was attributed to the dehalogenation pathway newly proposed in this study, successfully closing halogen balance during HAL degradation. In addition, a quantitative structure-activity relationship (QSAR) model was established for HAL degradation and the degradation rate constants for three mono-HALs were predicted at different temperature. The kinetic models and reaction rate constants obtained in this study can be used for quantitative predictions of HAL concentrations in drinking water, which is beneficial for monitoring and control of these emerging DBPs. Furthermore, considering the rapid degradation of Br-HALs into corresponding products, the temperature during sample pre-treatment can have a significant impact on DBP analysis., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

With the increasing discharge of wastewater effluent to natural waters, there is an urgent need to achieve both pathogenic microorganism inactivation and the mitigation of disinfection by-products (DBPs) during disinfection. Studies have shown that two-step chlorination, which injected chlorine disinfectant by splitting into two portions, was more effective in inactivating Escherichia coli than one-step chlorination under same total chlorine consumption and contact time. In this study, we observed a substantial reduction in the formation of five classes of CX 3 R-type DBPs, especially highly toxic haloacetonitriles (HANs), during two-step chlorination of secondary effluent when the mass ratio of chlorine-to-nitrogen exceeded 2. The shift of different chlorine species (free chlorine, monochloramine and organic chloramine) verified the decomposition of organic chloramines into monochloramine during second chlorination stage. Notably, the organic chloramines generated from the low molecular weight (< 1 kDa) fraction of dissolved organic nitrogen in effluent organic matter tended to decompose during the second step chlorination leading to the mitigation of HAN formation. Furthermore, the microbiological analysis showed that two-step chlorinated effluent had a slightly lower ecological impact on surface water compared to one-step chlorination. This work provided more information about the two-step chlorination for secondary effluent, especially in terms of organic chloramine transformation and HAN control., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

Changes in the activated sludge performance in an anaerobic/aerobic biological treatment system for leachate was discussed under the condition of tetracycline (TC) exposure. The results show that a low concentration of TC did not have an obvious effect on the removal of chemical oxygen demand (COD) while a high concentration of TC had a certain promoting effect. Under the stimulation of TC, the particle size distribution of anaerobic/aerobic sludge tended to be more uniform, the particle size of anaerobic sludge decreased while the settleability increased; however, the particle size of aerobic sludge increased due to bulking. With the addition of TC, the concentration of most heavy metal ions in sludge samples increased.TC exposure results in the release of a large amount of extracellular polymeric substances (EPS), thus leading to a smoother surface of anaerobic sludge and a rougher surface of aerobic sludge. The high removal efficiency of COD under the high concentration of TC was also presumed to be due to EPS promoting the microbial absorption of anaerobic substances in the leachate. The results clearly showed that TC had a bacteriostatic effect. After antibiotic exposure, the abundance and diversity index of bacteria in each reactor decreased obviously, the microbial community evolved, and the dominant species at the genus and phylum levels of anaerobic/aerobic reactors changed. This study provides a better understanding the effect of TC on activated sludge and has reference value for the management of antibiotic exposure in leachate treatment facilities.

Total organic halogen (TOX) in drinking water provides a measurement of the overall organic halogenated disinfection by-products (DBPs) formed during disinfection. Yangtze River Delta is one of the regions with the highest population density, the fastest urbanization process, and the most severe water pollution in China. Collecting water samples from full-scale drinking water treatment plants (DWTPs) in this region, this study firstly surveyed TOX occurrence in drinking water. Besides, the correlation of TOX formation potential (TOXFP) and trihalomethane formation potential (THMFP) with general water quality parameters (e.g., dissolved organic carbon [DOC], UV 254 , and specific ultraviolet absorbance) and the removal efficiencies of TOX precursors by different water treatment processes were also investigated. TOX levels in DWTP effluents (i.e., finished water) ranged from 29 to 165 μg/L (median 67 μg/L), and those in simulated distribution system waters ranged from 101 to 276 μg/L (median 158 μg/L). There were generally higher linear regression coefficient values for raw water (R 2  = 0.51-0.88) than for treated water (R 2  = 0.33-0.64) in terms of the relationship between DBP formation potentials and general parameters. However, a relatively stronger correlation between THMFP and TOXFP was observed for treated water (R 2  = 0.80, p < 0.001) than for raw water (R 2  = 0.64, p < 0.001). The overall treatment efficiencies of investigated parameters in DWTPs generally followed the order of UV 254  > DOC > TOX precursors > THM precursors. Notably, the overall removal rates of DOC and TOX precursors in summer (averaging 59 % and 54 %, respectively) were obviously higher than those in winter (averaging 39 % and 38 %, respectively), which was assumed to be related to the seasonal variation of bioactivity in sand filter. These results could expand the knowledge of TOX in drinking water, and provide valuable perspectives to water industry and DBP research., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

Microplastics are small plastic fragments that are of increasing concern due to their potential impacts on the environment and human health. The source of microplastics is not completely clear and might originate in daily lives such as from toothbrushes. When toothbrushes are used to clean teeth, small plastic debris and fragments can be potentially released into mouths directly or environment indirectly. This study aims to examine the release of microplastics from toothbrushes, using Raman imaging to identify and visualise the plastic debris with an increased signal-noise ratio via hyper-spectrum analysis. Using algorithms to convert the hyper-spectrum to an image, the plastic can be distinguished from the co-formulated titanium oxide particles that are not uniformly distributed along the plastics. The non-uniform distribution can lead to the bias results if a single spectrum analysis is conducted at one position rather than imaging analysis to scan an area. The potential false image originating from the off-focal position for the confocal Raman is overcome using the terrain map to guide the Raman imaging. The imaging analysis balancing between the low magnification to capture the overview and the high magnification to test the details is also discussed. While the release amount of microplastics from the toothbrush is estimated at thousands daily with the expected variation, the results of this study have confirmed the release of microplastics in daily lives. The imaging analysis approach along with algorithm can help to identify the chemical elements of microplastics from the complex background, which can benefit the further research on microplastics towards risk assessment and remediation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.)

The pH of chlorination is an important factor affecting the formation of disinfection byproducts (DBPs). In this study, we discovered that the genotoxicity induced by chlorination can be effectively reduced under alkaline conditions. As the pH of chlorination increased from 6.5 to 8.5, the genotoxicity of investigated waters reduced by ∼30-90 %. By assessing the genotoxicity of the mixture of measured DBPs, it was found that the contribution of measured DBPs to the overall genotoxicity was lower than 5 %, and the significant reduction of genotoxicity was largely associated with unknown DBPs. The result of Pearson's correlation analysis indicated that humified organics and soluble microbial byproducts were likely responsible for the genotoxicity, and their derived genotoxic compounds (i.e., unknown DBPs) tended to decompose during alkaline chlorination. However, the control of genotoxicity by alkaline chlorination was achieved at the expense of promoting trihalomethane (THM) formation. The highest genotoxicity reduction (93 %) was observed for chlorinated granular activated carbon-treated waters, but the formation of THMs was promoted to a level approaching that in untreated waters. The inconsistent trend of overall genotoxicity and THM concentration during alkaline chlorination suggested the inadequacy of THMs as metric for DBP exposure, and considerations should also be given to the toxicity of bulk water in addition to regulated DBPs., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

Microplastics (MPs) pollution is a pressing environmental issue for aquatic ecosystems. Landfill leachate is an important contributor of MPs and antibiotic resistant genes (ARGs). However, there are few studies on the colonization of ARGs and pathogens on MPs in leachate. This study conducted incubation experiments with polyethylene terephthalate (PET) and polypropylene (PP) MPs in landfill leachate which were about 3-5 years old (PL) and 5-10 years old (AL). After incubation, the bacterial cells colonized and grew on the surface of MPs, inducing the increase of oxygenated oxygen functional groups (e.g., hydroxyl, carbonyl) on the MPs surface. Real-time PCR indicated that MPs selectively enriched ARGs, such as genes tetM, tetC, mcr-1, aac(6')-Ib-cr, blaTEM and blaSHV in leachate. The diversity of bacterial communities on MPs was significantly increased in AL leachate, but decreased in PL leachate. The differences in bacterial communities in MPs biofilms were related to the type of MPs. Compared with AL leachate, the abundance of Chloroflexi increased by 15.7% on the PET, and the abundance of Acidobacteriota increased by 6.23 fold on the PP. The abundance of Firmicutes increased from 20.7% in PL leachate to 65.8% and 60.7% on PET and PP, respectively. Additionally, pathogens were observed to be more abundant on MPs compared to leachate. In particular, pathogens (Staphylococcus, Streptococcus, Enterobacter and Rhodococcus) associated with sul1 and sul2 were generally present at higher levels on MPs than in the surrounding leachate. These results provide significant implications for understanding the health risk of MPs in the environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Sandstorms, a natural meteorological event, occur repeatedly during the dry season and can accumulate large amounts of natural/anthropogenic pollutants during the deposition process, potentially introducing disinfection by-product (DBP) precursors into surface waters. In this study, the characteristics of sandstorm-derived dissolved organic matter (DOM) and its DBP formation potential were elucidated. Overall, sandstorm-derived DOM mainly consisted of low-molecular-weight, low-aromaticity, high-nitrogen organic matter, with a dissolved organic carbon (DOC) release yield of 14.4 mg-DOC/g. The halogenated DBP formation potential (calculated as total organic halogen) of sandstorm-derived DOM was comparable to that of surface water, while the normalized DBP-associated toxicity was 1.96 times higher. Similar to DOM introduced by other depositional pathways, sandstorm-derived DOM also had higher yields of highly cytotoxic DBPs (haloacetaldehydes [HALs], haloacetonitriles [HANs] and halonitromethanes [HNMs]). The average atmospheric deposition flux for DOM during the sandstorm event (50.4 ± 2.1 kg km -2 day -1 ) was 6.95 times higher than that of dry deposition, indicating a higher probability of contaminant input. Simultaneously, the estimation revealed that the sandstorm will increase the formation potential of toxicity forcing agents, such as HALs, HANs and HNMs, in surface water by 3.87%, 2.39% and 9.04%, respectively. Considering the high frequency of sandstorm events and the sorption of other organic pollutants by sand and dust, the impact of sandstorms on surface water quality should be of concern., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Plastic nanoparticles formed from both daily use of plastics and their wastes have emerged as a potential health and environmental hazard. It is necessary to study the biological process of nanoplastics in ecological risk assessment. To address this concern, we quantitatively investigated the accumulation and depuration of polystyrene nanoplastics (PSNs) in the tissues of zebrafish after the aquatic exposure using a quantitative method based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). Via the PSNs-spiked freshwater, zebrafish were exposed to three different concentrations of PSNs for 30 days, followed by 16 days of depuration. The results showed that the amounts of PSNs accumulated in zebrafish tissues were in the following order: intestine > liver > gill > muscle > brain. The uptake and depuration of PSNs in zebrafish both followed pseudo-first-order kinetics. It was revealed that the bioaccumulation was concentration, tissue and time dependent. When the PSNs concentration is low, the steady state might take longer time (or not occur) than that of a high concentration. After 16 days of depuration, there were still some PSNs present in the tissues particularly in the brain, where it might take 70 days or more to remove 75 % of PSNs. Overall, this work offers important knowledge on the bioaccumulation of PSNs, which may be useful for future studies into the health hazards of PSNs in aquatic environments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Advanced oxidation processes (AOPs) based on ultrasound (US) have attracted considerable attention in recent years due to its advantages in the degradation of landfill leachate. The review summarizes the existing treatment methods of leachate from lab-scale, compares their advantages and disadvantages by focusing on the degradation of emerging contaminants (ECs) in the leachate. Then the US-based AOPs are introduced emphatically, including their degradation mechanisms, influencing factors, energy consumption, further optimization methods as well as the possibility of field-scale application are systematically described. Moreover, this review also expounds on the advantages of dual-frequency US (DFUS) technology compared with single-frequency US, and a theoretically feasible DFUS process is proposed to treat ECs in the leachate. Finally, suggestions and prospects for US technologies in treating landfill leachate are put forward to aid future research on landfill leachate treatment. Meaningfully, this manuscript will provide reference values of US-based technologies in landfill leachate treatment for the practical use, facilitating the development of US-based AOPs in landfill leachate management and disposal., Competing Interests: Declaration of Competing Interest On behalf of the authors declare that, we have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)

Heavy metal pollution caused by industrial wastewater such as mining and metallurgical wastewater is a major global concern. Therefore, this study used modified lignite as a low-cost adsorbent for heavy metal ions. Pingzhuang lignite was dissolved and modified using Fusarium lignite B3 to prepare a biotransformed-lignite adsorbent (BLA). The O, H, and N contents of the BLA increased after transformation, and the specific surface area increased from 1.81 to 5.66 m 2 ·g -1 . Various adsorption properties were investigated using an aqueous solution of Cu(Ⅱ). The kinetic and isothermal data were well-fitted by pseudo-second-order and Langmuir models, respectively. The Langmuir model showed that the theoretical Cu(II) adsorption capacity was 71.47 mg·g -1 . Moreover, large particles and a neutral pH were favorable for the adsorption of heavy metal ions. The adsorption capacities of raw lignite and BLA were compared for various ions. Microbial transformation greatly improved the adsorption capacity, and the BLA had good adsorption and passivation effects with Cu(II), Mn(II), Cd(II), and Hg(II). Investigation of the structural properties showed that the porosity and specific surface area increased after biotransformation, and there were more active groups such as -COOH, Ar-OH, and R-OH, which were involved in the adsorption performance.

The effect of hydraulic parameters of an anaerobic/anoxic/oxic leachate treatment reactor on the removal of di(2-ethylhexyl) phthalate (DEHP) from aged landfill leachate was studied. The mean DEHP removal efficiencies were 79.5%, 87.1%, 89.7% and 87.8% at hydraulic retention times of 6, 4.5, 3 and 2 d, respectively. The removal efficiency of DEHP was significantly higher when the internal reflux ratio was 200% than others. There was no significant difference among the DEHP removal efficiencies at different external reflux ratios of the reactor. Due to the overall efficiency of the reactor, hydraulic retention time 3 d, internal reflux ratio 200% and external reflux ratio 60%, were considered the optimal hydraulic parameters for DEHP removal from aged leachate. The removal efficiency of DEHP was significantly improved (from 75.7% to 89.1%) after the optimization of hydraulic parameters of the reactor. The removal percentages of DEHP in the anaerobic, anoxic, and oxic units of the reactor were 42.8%, 17.6%, and 15.3%, respectively. The oxic microcosms in the reactor had little effect on DEHP removal. The correlation between DEHP and leachate pollutants indicated that DEHP removal was strongly correlated with leachate COD and NH 4 + -N.

Per- and polyfluoroalkyl substances (PFAS) are chemically and thermally stable due to the presence of carbon-fluorine (C-F) bond in their molecular structures, hence have been previously formulated as firefighting ingredients. During the firefighting process, however, owing to the high temperature, PFAS can be potentially degraded, particularly for PFAS precursors that contain non-C-F bonds, which is studied herein by exposing PFAS-contaminated soil in a muffle furnace oven. Different temperatures and time intervals are applied to the real soil sample to mimic the firing process and to evaluate the degradation and conversion of PFAS. This thermal treatment can not only degrade precursors (e.g. 6:2 fluorotelomer sulphonate), but also degrade perfluoroalkyl carboxylates (PFCA, e.g. perfluorooctanoic acid PFOA) and perfluoroalkyl sulfonates (PFSA, e.g. perfluorooctane sulfonate PFOS). The concentration dependence of the PFAS on temperature and time is fitted using a 2D Gaussian surface to simulate the complex thermal kinetic, and to compare with the traditional approach such as thermogravimetric analysis (TGA) (1D dependence on temperature only). The 2D simulation can directly visualise the thermal kinetic of individual or sum PFAS in the complex temperature-time plane, which depends on the sample background and particularly on the coexist PFAS precursors. Overall, this study provides a simple approach to monitor and optimise the thermal treatment of the PFAS-contaminated soil., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Per-and polyfluoroalkyl substances (PFAS) remediation is still a challenge. In this study, we propose a hybrid system that combines electrochemical treatment with ultrasound irradiation, aiming for an enhanced degradation of PFAS. Equipped with a titanium suboxide (Ti 4 O 7 ) anode, the electrochemical cell is able to remove perfluorooctanoic acid (PFOA) effectively. Under the optimal conditions (50 mA/cm 2 current density, 0.15 M Na 2 SO 4 supporting electrolyte, and stainless steel/Ti 4 O 7 /stainless steel electrode configuration with a gap of ∼10 mm), the electrochemical process achieves ∼100 % PFOA removal and 43 % defluorination after 6 h. Applying ultrasound irradiation (130 kHz) alone offers a limited PFOA removal, with 33 % PFOA removal and 5.5 % defluorination. When the electrochemical process is combined with ultrasound irradiation, we observe a significant improvement in the remediation performance, with ∼100 % PFOA removal and 63.5 % defluorination, higher than the sum of 48.5 % (43 % achieved by the electrochemical process, plus 5.5 % by the ultrasound irradiation), implying synergistic removal/oxidation effects. The hybrid system also consistently shows the synergistic defluorination during degradation of other PFAS and the PFAS constituents in aqueous film forming foam (AFFF). We attribute the synergistic effect to an activated/cleaned electrode surface, improved mass transfer, and enhanced production of radicals., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Numerous plastic items are known to gradually degrade and release microplastics and nanoplastics under certain conditions, which can be significantly accelerated by fire combustion. Unfortunately there is a limited knowledge about this burning process because the characterisation on microplastics and nanoplastics is still a challenge. In this study, an outdoor plastic chair is subjected to a combustion process, the change in the surface functional groups (due to different degree of burning) and the release of microplastics and nanoplastics are investigated. During the combustion process, the plastic is molten, burned and deposited on solid surfaces including concrete, stone and glass. Scanning electron microscopy (SEM) results show that the peeling off the deposited plastic generates a large number of fragments. Through Raman imaging, these fragments are characterised as polypropylene (PP) microplastics and nanoplastics due to appearance of characteristic peaks. To further increase the sensitivity, several algorithms are tested and optimised, including logic-based, non-supervised principal component analysis (PCA)-based, algebra-based and their hybrids (to intentionally correct the non-supervised PCA) to enable the effective extraction of the key information towards plastics characterisation, particularly by distinguishing the signal from the background noise towards the visualisation of the different degrees of burning. Based on the findings from Raman imaging and SEM, it is estimated that tens of microplastics and nanoplastics are created per μm 2 . Overall Raman imaging can be a suitable approach to characterise the microplastics and nanoplastics in a complex background, such as the fire-burned plastic items., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Plastic contamination is a growing global concern, but the characterisation approaches for microplastics are limited so far, and even more lacking for nanoplastics. As another public concern, bushfire has the potential to exacerbate the negative ecological effects of plastic waste. We thus study the release of microplastics and nanoplastics from toner powers printed on a paper sheet following a mimicked bushfire. The results show that, along the fire frontier, there is a charred area first, then a cindered area towards mineralisation via a full combustion. We find that, depending on the extent of burning, the printed toner powers containing microplastics can melt to aggregate, or crack to break down to nanoplastics, which are well characterised by mass spectrometry and Raman imaging combined with algorithms. Overall, the results shed new light on the microplastics and nanoplastics once affected by bushfire., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier B.V.)

Methyl parathion (MP) as an organophosphorus pesticide has been used in the control of agricultural pests and diseases. Due to its high toxicity and persistence in the environment, MP may pose threat to human health when it is released into environmental water. For MP treatment, people have found that oxidative degradation of MP may generate some intermediates which are more toxic than MP itself, such as methyl paraoxon. Herein, we proposed a new method of applying dielectric barrier discharge (DBD) non-thermal plasma technology to treat MP in aqueous solution, and investigated the influences of different gases, pH value, discharge voltage/power, and main active species on the MP removal efficiency. In particular, the safety of DBD treatment was concerned with analysis of the biological toxicity of the byproducts from the DBD oxidation, and the DBD-induced degradation together with the involved mechanism was explored therein. The results showed that the production of toxic intermediates could be effectively suppressed or avoided under certain treatment conditions. As such, this work demonstrates that the proper application of DBD plasma technology with necessary caution can detoxify methyl parathion effectively, and also provides a practical guide for low-temperature plasma application in treatment of various organophosphorus pesticides in agricultural wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Microplastics and antibiotics are common, typical pollutants, and they can cause compound pollution where they coexist in the environment. Surfactants in the environment can change the interface characteristics of pollutants, and then drive the change of environmental behavior of pollutants. In this paper, we studied the physicochemical properties of complexes of polystyrene (PS) and polyethylene (PE) contaminated with sodium dodecyl benzene sulfonate (SDBS); the complexes are referred to as SPS and SPE, respectively. Taking oxytetracycline (OTC) and norfloxacin (NOR) as representatives of broad-spectrum antibiotics, the effects of SDBS on the adsorption behavior of PS and PE were analyzed and possible mechanisms were proposed. The results showed that SDBS could effectively combine with PS and PE to enhance the surface electronegativity and reduce the Brunner-Emmett-Teller (BET) specific surface area and porosity. The crystal structure remained basically unchanged, and the surface functional groups changed slightly. SDBS greatly enhanced the saturated adsorption capacities of PS and PE for OTC and NOR, and made adsorption easier, which reduced the Gibbs free energy of the adsorption system. The adsorption behaviors of SPS and SPE for the two antibiotics were consistent with the Elovich kinetic model and Sips isothermal model. SDBS enhanced the hydrophilicity of the microplastics, which facilitated their adsorption of antibiotics dissolved in water. SDBS could directly combine with antibiotics to form a complex, further increasing the adsorption capacity of the microplastics for antibiotics. The -SO 3 H in SDBS could combine with oxygen-containing functional groups and -NH 2 in OTC and NOR. Non-ionic covalent bonds, electrostatic interactions, and hydrophobic attraction between the alkyl chain and benzene ring also played a role in adsorption. SDBS made it possible for MPs to load more types and quantities of pollutants and change their preferential adsorption selectivity, which significantly aggravated the environmental hazards., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Raman imaging can effectively characterise microplastics and nanoplastics, which is validated here to capture the items released from the plastic gloves when subjected to a mimicked fire. During the COVID-19 pandemic, large quantities of personal protective equipment (PPE) units have been used, such as the disposable gloves. If discarded and poorly managed, plastics gloves might break down to release secondary contaminants. The breakdown process can be accelerated by burning in a bushfire or at the incineration plants. During the burning process, the functional groups on the surface can be burned differently due to their different thermal stabilities. The different degrees of burning can be distinguished and visualised via Raman imaging. In the meantime, at the bottom of the burned plastics, microplastics and nanoplastics can be generated at a significant amount. The possible false Raman imaging on microplastics and nanoplastics is also discussed, by effectively extracting and distinguishing the weak signal from the background or noise. Overall, these findings confirm the importance of effectively working waste incineration plants and litter prevention, and suggest that Raman imaging is a suitable approach to characterise microplastics and nanoplastics., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Microplastics (MPs) could serve as vectors of antibiotics and heavy metals through sorption and desorption. However, the combined adsorption process of antibiotics and heavy metals on aged MPs has rarely been studied. In this study, combined adsorption/desorption of tetracycline (TC) and Cd(II) on/from polystyrene (PS) and polyethylene terephthalate (PET) MPs, as well as ultraviolet (UV) and H 2 O 2 aged MPs, was investigated. The specific surface areas of the MPs increased after UV and H 2 O 2 aging. Adsorption experiments showed that the pseudo-second-order kinetic model and Freundlich model fitted adsorption of TC and Cd(II) on all of the MPs. The adsorption capacities of TC and Cd(II) were higher on aged MPs than on the pristine MPs, especially on H 2 O 2 treated MPs. TC adsorption on the MPs was hardly affected by Cd(II), and Cd(II) adsorption was not significantly affected by TC when the solution pH value was below 8.0. Cd(II) slightly enhanced TC adsorption on the MPs at pH 8.0, especially on the aged MPs. The TC adsorption capacities increased with increasing pH, reaching a maximum at pH 5.0 or 6.0, and they then decreased, while the largest level of Cd(II) adsorption was at approximately pH 6.0. Adsorption of TC and Cd(II) on the pristine and aged MPs was thermodynamically favorable and spontaneous. The trend of the desorption rates of TC and Cd(II) from the MPs in different background solutions was ultrapure water < surface water < simulated gastric fluid. The desorption rates of TC and Cd(II) from the aged MPs were lower than those from the pristine MPs. The results revealed the mechanism of the TC and Cd(II) combined adsorption process on aged MPs, which will provide insight for understanding the aging process and its potential effects on sorption and desorption of antibiotics and heavy metals in the real environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Snow with large specific surface area and strong adsorption capacity can effectively adsorb atmospheric pollutants, which could/might lead to the increase of disinfection by-product (DBP) precursors in surface water. In this study, the contents and characteristics of dissolved organic matter (DOM) in meltwater were investigated, and DBP formation and the DBP-associated cytotoxicity index during chlorination of meltwater was first explored. Overall, meltwater exhibited high nitrogen contents. Meltwater-derived DOM was mainly composed of organics with low molecular weights, low aromaticity, and high unsaturated degrees. DBP formation potentials and cytotoxicity indexes in chlorinated meltwater were positively correlated with air quality index and were significantly impacted by snowfall stages. The trihalomethane and haloacetic acid yields from meltwater were relatively low, while yields of highly cytotoxic DBPs, especially halonitromethanes (6.3-10.8 μg-HNMs/mg-DOC), were significantly higher than those of surface water (1.7 μg-HNMs/mg-DOC). Notably, unsaturated nonaromatic organic nitrates in meltwater were important precursors of halonitromethanes. The actual monitoring results showed that snowfall significant increased the haloacetaldehydes and nitrogenous DBP formation levels of surface water. Considering increased DBP formation and DBP-associated toxicity, it was demonstrated that DOM derived from snowfall in atmosphere-polluted areas could deteriorate surface water quality and pose potential risks to drinking water.

Due to COVID-19, large amounts of personal protective equipment (PPE) have been used, and many PPE units are made of plastics, such as face masks. The masks can be burned naturally in a bushfire or artificially at the incineration plants, and release microplastics and nanoplastics from the mask plastic fibres. A fire can cause the plastic, such as polypropylene (PP) fibres, to be molten and stick to the solid surface, such as glass, soil, concrete or plant, as films or islands, due to the binding property of the molten plastic material. Once the films or islands are peeled off in the processes such as weathering, ageing, or treatment and clean-up, there are residuals leftover, which are identified as nanoplastics and microplastics via Raman imaging, with the significant release amount of ~1100 nanoplastics / 10 µm 2 or ~11 billion / cm 2 , and ~50 microplastics / 420 µm 2 or ~12 million / cm 2 . Moreover, surface group is deviated on the plastic surface, which can also be distinguished and visualised as well via Raman imaging, down to nano size. This test validates the Raman imaging approach to capture microplastics and nanoplastics, and also provides important information about the fate and transportation of PPE mask in the environment, particularly when subjected to a fire. Overall, Raman imaging can be an effective option to characterise the microplastics and nanoplastics, along with the deviated surface group., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Microplastics (MPs), due to their impacts on the ecosystem and their integration into the food web either through trophic transfer or ingestion directly from the ambient environment, are an emerging class of environmental contaminants posing a great threat to marine organisms. Most reports on the toxic effects of MPs exclusively focus on bioaccumulation, oxidative stress, pathological damage, and metabolic disturbance in fish. However, the collected information on fish immunity in response to MPs is poorly defined. In particular, little is known regarding mucosal immunity and the role of mucins. In this study, marine medaka (Oryzias melastigma) larvae were exposed to 6.0 µm beads of polystyrene microplastics (PS-MPs) at three environmentally relevant concentrations (10 2 particles/L, 10 4 particles/L, and 10 6 particles/L) for 14 days. The experiment was carried out to explore the developmental and behavioural indices, the transcriptional profiles of mucins, pro-inflammatory, immune, metabolism and antioxidant responses related genes, as well as the accumulation of PS-MPs in larvae. The results revealed that PS-MPs were observed in the gastrointestinal tract, with a concentration- and exposure time-dependent manner. No significant difference in the larval mortality was found between the treatment groups and the control, whereas the body length of larvae demonstrated a significant reduction at 10 6 particles/L on 14 days post-hatching. The swimming behaviour of the larvae became hyperactive under exposure to 10 4 and 10 6 particles/L PS-MPs. In addition, PS-MP exposure significantly up-regulated the mucin gene transcriptional levels of muc7-like and muc13-like, however down-regulated the mucin gene expression levels of heg1, muc2, muc5AC-like and muc13. The immune- and inflammation and metabolism-relevant genes (jak, stat-3, il-6, il-1β, tnf-а, ccl-11, nf-κb, and sod) were significantly induced by PS-MPs at 10 4 and 10 6 particles/L compared to the control. Taken together, this study suggests that PS-MPs induced inflammation response and might obstruct the immune functions and retarded the growth of the marine medaka larvae even at environmentally relevant concentrations., (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)

Disinfection by-products (DBPs), formed from the reactions of disinfectants with natural organic matter and halides in drinking water, were considered to be cytotoxic and genotoxic, and might trigger various cancers. The relatively low concentration of DBPs in finished water (low µg/L or even ng/L levels) and the interference from water matrix inhibited in situ determination of DBPs. Moreover, the further formation and degradation of DBPs by disinfectants during the holding time (several hours to several days) from sample collection to analysis could adversely affect the determination of DBPs. To obtain accurate, precise and reliable data of DBP occurrence and formation, robust and reliable sample preservation is indispensable. However, the commonly used quenching agents (e.g., sodium sulfite, sodium thiosulfate, and ascorbic acid) for sample preservation can decompose reactive DBPs by reductive dehalogenation. This study evaluated the performance of N-acetylcysteine (NAC) and glutathione (GSH) as quenching agents for the analysis of halogenated DBPs by investigating the stoichiometry of the disinfectant-quenching agent reaction, the formation of DBPs during chlor(am)ination of NAC or GSH, and the effects of NAC or GSH on the stability of 18 individual DBPs and total organic halogen (TOX). Based on the results of this study, NAC and GSH were considered to be ideal quenching agents for the analysis of most DBPs and TOX, except halonitromethanes., (Copyright © 2022. Published by Elsevier B.V.)

Microplastics can be found almost everywhere, including in our kitchens. The challenge is how to characterise them, particularly for the small ones (<1 μm), referred to as nanoplastics, when they are mixed with larger particles and other components. Herewith we advance Raman imaging to characterise microplastics and nanoplastics released from a dish sponge that we use every day to clean our cookware and eating utensils. The scanning electron microscopy result shows significantly different structures of the soft and hard layers of the sponge, with the hard layer being more likely to shed particles. By scanning the sample surface to generate a spectrum matrix, Raman imaging can significantly improve signal-noise-ratio, compared with individual Raman spectra. Through mapping the characteristic peaks from the matrix that contains hundreds, even thousands of Raman spectra, it is confirmed that the particles released from the soft and hard layers of the sponge are mainly Nylon PA6 and polyethylene terephthalate, respectively. Using principal component analysis (PCA) to decode the spectrum matrix further enhances the signal-noise ratio, which enables mapping the whole set of the spectrum, rather than the selected peaks. By optimising the Raman scanning parameters, the PCA-Raman imaging is able to reliably capture and visualise microplastics and nanoplastics released from both sides of the dish sponge, including a plastic-surrounding-sand composite structure. Overall, PCA-Raman imaging is a holistic and effective approach to characterising miniature plastic particles., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

As contaminants of emerging concern, microplastics and nanoplastics are ubiquitous in not only aquatic and terrestrial environments but also household settings. While the characterisation of microplastics is still a challenge, the analysis of nanoplastics is even more difficult. In this study, we aim to examine several novel algorithmic methods intended for analysing complex Raman spectrum matrices towards visualisation of plastic particles released from a chopping board. Specifically, we compare and advance three decoding algorithms, including (i) a logic-based algorithm to merge and cross-check multiple Raman images that map the intensities of several characteristic peaks; (ii) a principal component analysis-based algorithm to generate intensity images from whole sets of spectra, not just from individual characteristic peaks; (iii) an algebra-based algorithm to merge and cross-check the loading matrix to enhance characterisation efficiency. Assisted with a scanning electron microscope, we estimate that 100-300 microplastics / nanoplastics per mm per cut along the groove formed on the chopping board, and ~3000 per mm 2 per cut in the scratched area, may be released from a chopping board during food preparation and may be subsequently ingested by human. Overall, the Raman imaging combined with algorithms can provide effective characterisation of microplastics and nanoplastics., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Landfill leachate has a high chloride (Cl - ) content. Because it is highly mobile, and cannot be sorbed or transformed bio-chemically, it is important to have detailed information about how it migrates in landfill sites. In this study, we set up four lab-scale simulated landfills, including an anaerobic landfill (AL), an anaerobic landfill with leachate recirculation (RAL), an anaerobic/semi-anaerobic landfill with leachate recirculation (RASL), and an anaerobic/semi-aerobic landfill (ASL), to explore how, when regulated, moisture and air affected the migration of chlorine. We found that water and air had a strong influence on the release of Cl - . Leachate obviously promoted Cl - dissolution in refuse when recirculated. When air was introduced into landfill, thereby changing it from anaerobic to semi-aerobic, the leachate Cl - concentration increased sharply from around 4-9 g L -1 (RASL) and 18 g L -1 (ASL), respectively. In principle, Cl - is released continuously when leachate is recirculated in landfills (RAL and RASL), but it can also be found a terminal when the leachate recirculation stops (AL and ASL). Cumulative amounts of 64, 66, 27, and 53 g of Cl - were released from the AL, RAL, RASL, and ASL, respectively. Lower COD/Cl and N H 4 + -N/Cl ratios in ASL and RASL after day 175 indicated that lower Cl - pollution risk than that in AL and RAL.

Landfill leachate is an important source and sink of antibiotics and antibiotic resistance genes (ARGs), which poses a potential threat to human health and ecological environment. Ten antibiotics and 8 ARGs in leachates collected from Zhejiang Province, China, were systematically investigated. The effects of multiple factors were considered: leachate age, season when the leachate was sampled (dry or rainy), heavy metal concentrations, and leachate quality parameters. Leachate age was crucial to the profile of the detectable antibiotics and ARGs. The total concentration of antibiotics were in the order of macrolides > sulfonamides > tetracyclines and they decreased significantly with leachate age. Similarly, fewer ARGs were harbored in aged leachate; the order of abundance of the ARGs was mexF (11.92 ± 0.22 log 10 gene copies/L) > sul2 > Intl1 > sul1 > ermB > mefA > tetM > tetQ (9.57 ± 1.32 log 10 gene copies/L). The extreme abundances (i.e., the maxima and minima) of ARGs relating to the same class of antibiotic were always surprisingly similar and appeared in leachate of the same age. Seasonal variation greatly affected the concentrations of antibiotics in the leachate-the concentration difference between the dry and rainy seasons could reach two orders of magnitude. Heavy metal concentrations and leachate quality parameters also had important effects on the distribution of antibiotics and ARGs. Overall, the profile of antibiotics and ARGs in leachates was influenced by numerous factors, and the pollution of antibiotics and ARGs may be reduced and controlled by adjusting the environmental factors., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The characterisation of nanoplastics is much more difficult than that of microplastics. Herewith we employ Raman imaging to capture and visualise nanoplastics and microplastics, due to the increased signal-noise ratio from Raman spectrum matrix when compared with that from a single spectrum. The images mapping multiple characteristic peaks can be merged into one using logic-based algorithm, in order to cross-check these images and to further increase the signal-noise ratio. We demonstrate how to capture and identify microplastics, and then zoom down gradually to visualise nanoplastics, in order to avoid the shielding effect of the microplastics to shadow and obscure the nanoplastics. We also carefully compare the advantages and disadvantages of Raman imaging, while giving recommendations for improvement. We validate our approach to capture the microplastics and nanoplastics as particles released when we cut and assemble PVC pipes in our garden. We estimate that, during a cutting process of the PVC pipe, thousands of microplastics in the range of 0.1-5 mm can be released, along with millions of small microplastics in the range of 1-100 μm, and billions of nanoplastics in the range of <1 μm. Overall, Raman imaging can effectively capture microplastics and nanoplastics., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The spatial distribution and composition of microplastics in near-surface water (8 m) was investigated from the East Asian Seas to the Arctic Central Basin. Microplastics were detected in 93.9% of the sampling sites. Abundances ranged from 0.48 to 7.62 items/m 3 , with an average abundance of 2.91 ± 1.93 items/m 3 . The highest average abundance was observed in the Arctic Central Basin. Polyester (PET) was the dominant type, accounting for 71.3% of total microplastics, followed by rayon or cellophane and polytetrafluoroethylene (PTFE). Microplastics < 2 mm accounted for 81.9% of total particles. Its distribution peaked in the 1-2 mm size range. The 0.30-2 mm fibers were the most abundant. In the East Asian Seas, the abundance was significantly negatively correlated with longitude, whereas the accumulation of microplastics was not observed in the northeastern sector of Japan Sea. Abundances of microplastics at sites located in the sub-Arctic and Arctic Oceans showed a significant positive relationship with latitude, indicating that the Arctic Ocean is a potential accumulation zone of microplastics. The findings of this study will provide systematical insights into distribution of microplastics and basic information for understanding the accumulation mechanism of microplastics in near-surface waters from the East Asian Seas to the Arctic Central Basin., Competing Interests: Declaration of competing interest No conflict of the interest exits in the submission of this revised manuscript, and manuscript is approved by all the authors for publication. This article is our original work, hasn't received prior publication and isn't under consideration for publication elsewhere., (Copyright © 2021. Published by Elsevier B.V.)

The characterisation of microplastics is still a challenge, and the challenge is even greater for nanoplastics, of which we only have a limited knowledge so far. Herewith we employ Raman imaging to directly visualise microplastics and nanoplastics which are released from the trimmer lines during lawn mowing. The signal-noise ratio of Raman imaging is significantly increased by generating an image from hundreds or thousands of Raman spectra, rather than from a single spectrum, and is further increased by combining with the logic-based and PCA-based algorithms. The increased signal-noise ratio enables us to capture and identify microplastics and particularly nanoplastics, including plastic fragments or shreds (with diameters / widths of 80 nm - 3 µm) and nanoparticles (with diameters of < 1000 nm) that are released during the mimicked mowing process. Using Raman imaging, we estimate that thousands of microplastics (0.1-5 mm), and billions of nanoplastics (< 1000 nm), are released per minute when a line trimmer is used to mow lawn. Overall, Raman imaging provides effective characterisation of the microplastics and is particularly suitable for nanoplastics., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Tetracycline is a common antibiotic and is often carelessly released into the natural environment, thus constantly posing potential threats to the environment. Currently, due to lack of effective methods to remove it from the environmental water system, researchers are still exploring new ways to deal with tetracycline. In this work, we employed atmospheric-pressure non-thermal plasma (NTP) to treat tetracycline in water and investigated the involved degradation mechanism. The enhanced degradation efficiency was acquired and investigated, and the degradation mechanism by the plasma-generated active species were explored. The tetracycline degradation pathways via especially the interactions with plasma-generated hydroxyl radical and ozone were examined by virtue of UV spectroscopy, three-dimensional fluorescence spectroscopy, high performance liquid chromatography-mass spectrometry (HPLC-MS), together with the assistance of theoretical simulations. Moreover, the toxicological evaluation of NTP treatment of tetracycline was also provided, which confirmed that the biological toxicity of tetracycline degradation products was negligible. Therefore, this work provides not only the effective way of treating antibiotics by engineered plasma technology, but also the insights into the mechanisms of degradation of antibiotics by NTP., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Microplastics can potentially be released in our daily activities, such as via our showers, as our clothes are made of plastic fibres, and/or cotton fibres. The challenge is how to characterise these microplastics in shower debris. Herewith we employ Raman imaging to directly visualise the microplastics collected from shower wastewater. Raman can map an image from the scanning array that contains a matrix of thousands of spectra, featuring a considerably higher signal-noise ratio than that from a single spectrum. The increased signal-noise ratio reduces the complexity of sample preparation. Consequently, after the shower debris was sampled and washed, Raman imaging allowed us to distinguish the microplastic fibres from the background including cotton fibres and dirt aggregates. Interestingly, by adjusting the laser power intensity, the scanning process enabled simultaneous in-situ bleaching of the colorants formulated in the textile fibres and collection of signals. The disadvantage of Raman imaging such as the short focusing/working distance is also presented and discussed. Overall, the Raman imaging can extract meaningful information from the complex shower debris samples to enable analysis of microplastics., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Monolithic carbon foams are promising materials for adsorption due to the easy recyclability and without secondary-pollution. However, poor adsorption efficiency for organic pollutants limits its practical application. Hence, this work proposed a novel monolithic porous carbon foam by a facile carbonization approach as freestanding electrodes to remove the organic dyes. The prepared carbon foam derived from waste cigarette filters and zeolitic-imidazolate frameworks-8 with well-developed pores, and the calculated surface area is 1457 m 2 ·g -1 , and exhibited an outstanding removal efficiency for methylene blue in aqueous. The maximum adsorption capacity for methylene blue can reach up to 1846.7 mg·g -1 under the applied voltage of -1.2 V. Importantly, as-prepared carbon foams possessed excellent stability, and the removal efficiency can remain above 85% after 5 cycles. Thus, obtained porous carbon foams in this paper as a free standing electrode is expected to be promising materials of adsorbent besides supercapacitors., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

There exist two common processes in fishery culture, i.e. antibiotic addition to reduce disease in fishery, and chlorination disinfection to inhibit infectious pathogenic microorganisms. However, antibiotic residues might play important reverse side roles for both aquaculture water pollution and potential formation of chlorination side products. Herein, the transformation behaviour, intermediates analyses and conversion pathway of antibiotic sulfamethoxazole (SMX), and potential generation of halogenated acetic acids (HAAs) in the process of chlorination in fishery water were examined, and the results revealed that the decomposing of SMX satisfied a pseudo first-order kinetic equation. Both the addition of available chlorine and high temperature had affirmative influences on the decontamination of SMX and production of HAAs, and the near-neutral pHs promoted the removal of SMX and generation of HAAs. Br - was favorable for the removal of SMX and yields of brominated acetic acids (Br-AAs). Based on the identified intermediate products, the transformation path of SMX in chlorination process was propounded, to wit, the C-S and S-N bonds in the SMX molecules were firstly cracked, and the primeval intermediate groups are then transformed to form chloroanilines, chlorophenols, etc., and subsequently, chlorophenols were chlorinated and ring-opened to generate toxic HAAs. This study might be meaningful to evaluate the effective removal of sulfonamide antibiotic residues and the potential generation of halogenated DBPs (H-DBPs) when chlorinated in aquaculture water., (Copyright © 2021. Published by Elsevier Inc.)

As emerging contaminants, microplastics are challenging to characterize, particularly when their size is at the nanoscale. While imaging technology has received increasing attention recently, such as Raman imaging, decoding the scanning spectrum matrix can be difficult to achieve result digitally and automatically via software and usually requires the involvement of personal experience and expertise. Herewith, we show a dual-principal component analysis (PCA) approach, where (i) the first round of PCA analysis focuses on the raw spectrum data from the Raman scanning matrix and generates two new matrices, with one containing the spectrum profile to yield the PCA spectrum and the other containing the PCA intensity to be mapped as an image; (ii) the second round of PCA analysis merges the spectrum from the first round of PCA with the standard spectra of eight common plastics, to generate a correlation matrix. From the correlation value, we can digitally assign the principal components from the first round of PCA analysis to the plastics toward imaging, akin to dataset indexing. We also demonstrate the effect of the data pretreatment and the wavenumber variations. Overall, this dual-PCA approach paves the way for machine learning to analyze microplastics and particularly nanoplastics.

Sediment has been considered as an important sink for microplastics (MPs), but there are limited reports about the spatial and temporal variability of MPs in sediment from the Arctic Ocean. Furthermore, understanding is lacking on the correlation between Arctic sea ice variation and MP abundance in sediment. This study aimed to assess the MP contamination in the sediment from the Chukchi Sea over five years through three voyages (in 2016, 2018, and 2020). The MP abundances in the sediments from the Chukchi Plateau and Chukchi Shelf over five years ranged from 33.66 ± 15.08 to 104.54 ± 28.07 items kg -1 dry weight (DW) and 20.63 ± 6.71 to 55.64 ± 22.61 items kg -1 DW, respectively. The MP levels from the Chukchi Sea were lower than those from the Eastern Arctic Ocean. Our findings suggest that the Chukchi Plateau is an accumulation zone for fibers related to fishing gear and textiles under the dual influence of the Pacific and Atlantic Ocean currents. However, the reduction of these fibers in the sediment from the Chukchi Shelf might be related to bottom currents, sediment resuspension, and biomass. Moreover, the MP abundance in the sediment from the Chukchi Sea was positively correlated with the reduction of Arctic sea ice, suggesting that the melting sea ice contributes to the increase in MP levels in the sediment. The increase in blue MPs from the Chukchi Plateau over time might be attributed to melting sea ice or intense fishing activity, whereas the increase of the smallest MPs in this region could be owing to the breakdown of larger plastics during long-distance transport or the easier settlement of smaller MPs. Further time-series investigations are urgently required to improve the understanding of the environmental fate and transport of MPs among the different Arctic environmental compartments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021. Published by Elsevier B.V.)

The wide presence of microplastics (MPs) in the ocean leads their exposure on marine fish. MP contamination was reported for the gastrointestinal tracts and gills of 117 marine fishes attributed to nine species from Xiamen Bay, a special economic zone in China. Among species, MP abundance ranged from 1.07 items individual -1 to 8.00 items individual -1 . Fibers dominated MP shapes, accounting for 59.03% of all MPs. Polymer composition was dominated by polyamide (26.97%) and rayon (17.56%). MPs were most commonly (55.22%) transparent, and most (77.61%) were < 1 mm in size. Our report represents the first of MP contamination in wild marine fish from Xiamen Bay, which we determine to be at an intermediate to slightly higher level compared with levels reported elsewhere, and provides further insights into potential risks of MPs pose to fish and human health., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Coagulation is well-established for controlling regulated disinfection by-products (DBPs), but its effectiveness for controlling unregulated DBPs remains unclear. The efficiency of coagulation in controlling unregulated DBPs requires clarification owing to their relatively high toxicity. In this study, three Al-based coagulants, aluminum sulfate (Alum), polyaluminum chloride (PAC), and a novel type of covalently bond hybrid coagulant (CBC, synthesized using AlCl 3 ) were selected, and the coagulation performance of these Al-based coagulants in controlling DBPs and DBP-associated toxicity was compared over 5 classes of DBPs, including trihalomethanes, haloacetic acids, haloacetaldehydes, haloacetonitriles, and halonitromethanes. The results showed that Alum was the least efficient in removing DBP precursors among the three coagulants. The effectiveness of CBC and PAC for DBP control varied with the characteristics of source waters. CBC had an advantage in water with a low content of humic acids, and reduced DBP concentration and DBP-associated toxicity by 47% and 25%, respectively. For water rich in aromatic organics, CBC might serve as DBP precursors at a high-required dosage, suggesting that a trade-off between enhanced DBP control and serving as DBP precursors should be considered for CBC coagulation; PAC achieved the most reduction in DBP concentration and DBP-associated toxicity by 50% and 34%, respectively., (Copyright © 2021. Published by Elsevier B.V.)

Microplastics are among the ubiquitous contaminants in our environment. As emerging contaminants, microplastics are still facing with lots of challenges on the characterisation, including their capture, identification and visualisation, particularly from a complex background. For example, when we print documents using a laser printer, we are printing microplastics onto paper, because the plastics are the main ingredient of the toner powder mixture. Characterisation of these microplastic mixture meets an even more complicated challenge, because plastic's signals might be shielded by other toner powder ingredients such as the pigments, the dyes, the black carbon, and the paper fabrics as well. To solve this challenge, we employ various techniques, including SEM, TEM, XPS, FT-IR, TGA and Raman, to characterise the microplastics printed via the toner powders. Interestingly, we show that Raman can distinguish and visualise the distribution of the microplastics from the complex background of the mixture. We estimate the millions of toner powders, each of which is ~4-6 μm in size, are printed out per A4 sheet as microplastics. The findings send a strong warning that millions of microplastics might be generated from the printing activities in our daily lives., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

The effects of hydraulic condition of reactor and the dominant degrading bacteria on the removal of di-n-butyl phthalate (DBP) from aged landfill leachate by anaerobic/anoxic/oxic (A/A/O) leachate treatment process were investigated. The optimal DBP removal (96.0%) was obtained from aged leachate when the hydraulic retention time (HRT) of the reactor was 3 d, internal reflux ratio of the reactor was 200%, and external reflux ratio of the reactor was 60%, respectively. The removal efficiency of DBP was significantly improved after the inoculation of the dominant DBP-degrading bacteria (Pseudomonas sp. W1) in the reactor. The mean removal efficiencies of DBP before and after inoculation were 94.1% and 97.7%, respectively. Furthermore, the inoculation of dominant DBP-degrading bacteria changed the original sludge structure and characteristics, which was more conducive to the removal of DBP. These results provide theoretical basis for the effective removal of DBP from aged leachate by the biological treatment process., (Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.)

The Yangtze River basin covers one-fifth of China's land area and serves as a water source for one-third of China's population. During long-distance water transport from upstream to downstream, various sources of dissolved organic matter (DOM) lead to considerable variation in DOM properties, significantly impacting water treatability and disinfection byproduct (DBP) formation after chlorination. Using size-exclusion chromatography and fluorescence spectroscopy, the spatial variation in DOM characteristics was comprehensively investigated on a basin scale. The formation of 36 DBPs and speciated total organic halogen in chlorinated samples was determined. Overall, the Yangtze River waters featured a high proportion of terrestrially derived humic substances that served as important precursors for trihalomethanes and haloacetic acids, which was responsible for the increase in total DBP formation along the Yangtze River. The downstream waters were characterized by high levels of microbially derived protein-like biopolymers, which significantly contributed to the formation of haloacetaldehydes and haloacetonitriles that dominated DBP-associated mammalian cell cytotoxicity. Moreover, the precursors of haloacetaldehydes and haloacetonitriles in downstream waters were highly hydrophilic, posing a challenge for water treatment. This study presents an extensive basin-scale study, providing insights into DOM variations along the Yangtze River, illustrating the impact of DOM properties on drinking water from a DBP perspective.

Marine biota, especially commercially important species, serves as a basis for human nutrition. However, millions of tons of plastic litter are produced and enter the marine environment every year, with potential adverse impacts on marine organisms. In the present study, we investigated the occurrence and characteristics of microplastic (MP) pollution in the digestive tracts of 13 species of wild nektons from 20 stations sampled in the South China Sea (SCS) and the Indian Ocean (IO), and assessed the human health risks of MPs. The detection rate of MPs ranged from 0.00% to 50.00% from the SCS, which was dramatically lower than that from the IO (10.00-80.00%). The average abundance of MP was 0.18 ± 0.06 items g wet weight -1 (ww -1 ) in the SCS, which was significantly lower than that in the IO with a concentration of 0.70 ± 0.16 items g ww -1 . Most MPs were fibers in type, black in color, and polyester (PES) in polymer composition in both the SCS and IO. Interestingly, distinct profiles of MP pollution were found between the benthic and pelagic nektons: 1) The predominant MP composition was PES in the benthic nektons, whereas polyamide (PA) accounted for a larger part of the total MP count in the pelagic nektons within the SCS; 2) The abundance of MP in the benthic nektons (0.52 ± 0.24 items individual -1 ) was higher than that in the pelagic nektons (0.30 ± 0.11 items individual -1 ). Accordingly, the mean hazard score of MPs detected in the benthic nektons (220.66 ± 210.75) was higher than that in the pelagic nektons (49.53 ± 22.87); 3) The mean size of the MP in the pelagic nektons (0.84 ± 0.17 mm) was larger than that in the benthic nektons (0.49 ± 0.09 mm). Our findings highlight the need to further investigate the ecological impacts of MPs on wild nekton, especially commercially important species, and its potential implications for human health., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Plastics have been recognized as a serious threat to the environment. Besides their own toxicity, microplastics can interact with other environmental pollutants, acting as carriers and potentially modulating their toxicity. In this study, the toxicity of polystyrene (PS) microplastic fragments (plain PS; carboxylated PS, PS-COOH and aminated PS, PS-NH 2 ) and triphenyl phosphate (TPhP) (an emerging organophosphate flame retardant) at the environmentally relevant concentrations to the marine medaka (Oryzias melastigma) larvae was investigated. Larvae were exposed to 20 μg/L of microplastic fragments or 20 and 100 μg/L of TPhP or a combination of both for 7 days. The results showed that the three microplastics did not affect the larval locomotor activity. For TPhP, the larval moving duration and distance moved were significantly decreased by the TPhP exposure, with a maximum decrease of 43.5% and 59.4% respectively. Exposure to 100 μg/L TPhP respectively down-regulated the expression levels of sine oculis homeobox homologue 3 (six3) and short wavelength-sensitive type 2 (sws2) by 19.1% and 41.7%, suggesting that TPhP might disturb eye development and photoreception and consequently the low locomotor activity in the larvae. Interestingly, during the binary mixture exposure, the presence of PS, PS-COOH or PS-NH 2 reversed the low locomotor activity induced by 100 μg/L TPhP to the normal level. Relative to the larvae from the 100 μg/L TPhP group, the movement duration and distance moved were increased by approximately 60% and 100%, respectively, in the larvae from the TPhP + PS, TPhP + PS-COOH and TPhP + PS-NH 2 groups. However, the gene expression profiles were distinct among the fish from the TPhP + PS, TPhP + PS-COOH and TPhP + PS-NH 2 groups, implying different mechanisms underlying the reversal of the locomotor activity. The findings in this study challenge the general view that microplastics aggravate the toxicity of the adsorbed pollutants, and help better understand the environmental risk of microplastic pollution., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Reverse osmosis (RO), a promising technology for removing inorganic salts and a wide range of trace organic pollutants, is widely used in water treatment industry. In this study, the rejection of chlorinated, brominated, and iodinated trihalomethanes (THMs) by a multi-stage RO system was investigated. The results showed that the multi-stage RO system is effective in rejecting THMs, and THMs with large size, high hydrophobicity and low polarity were highly rejected. In the first stage, high percentage of THMs was adsorbed on RO membrane, and the THM rejection was dominated by both hydrophobic adsorption and size exclusion. The contribution of hydrophobic adsorption to THM rejection decreased significantly along RO stages due to decreased feed concentration, but the enhancement of size exclusion still ensured high rejection efficiencies for most THMs, indicating a compensation effect between two rejection mechanisms. Finally, to further understand the rejection in the multi-RO system from a perspective of THM property, multiple linear regression models were built. The impact of n-octanol-water partition coefficient (Log K ow ) was slightly higher than that of stokes radius in the first stage, which was consistent with the rejection mechanism. But dipole moment played an increasingly important role in the second and third stage, weakening the impact of Log K ow on THM rejection., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

This study developed a facile approach for the fabrication of dual MgO-loaded carbon foam (DMCF) via carbonization of a cured MgO/cyanate ester resin mixture, which underwent self-foaming of the resin followed by the carbothermal reduction of MgO. The features of the prepared DMCF prepared were characterized by FESEM, TEM, XRD, FTIR, XPS and so on, and the effects of adsorption conditions, adsorption isotherms, kinetics, and thermodynamics on malachite green (MG) removal using the DMCF as adsorbents were investigated through batch adsorption experiments. Results demonstrate that the DMCF possesses a unique dual loading of MgO particles which are not only loaded onto its foam walls but also filled within the walls with a graphene-wrapped core-shell structure. The experimental maximum adsorption capacity of MG reaches up to 1874.18 mg/g with a partition coefficient of 10.87 mg/g/μM. The adsorption process can be better described with Langmuir, pseudo-second-order, and intraparticle diffusion models. Moreover, the DMCF exhibits a removal percentage of 84.85% after five reuses, indicating that it is an efficient and promising adsorbent for MG adsorption., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Landfill arsenic pollution is a complicated problem because of the sophisticated species and transformation of fractions involved. This study investigated arsenic transformation behavior from the viewpoint of arsenic functional genes based on analysis of 29 aged refuse samples collected from 11 sanitary landfills in 10 cities in Zhejiang Province, China. Arsenic species distribution varied significantly with landfill process. Landfill contains rich arsenic resistant microbes. arrA genes were the key factor responsible for arsenic transformation and migration in landfill. Although the abundance of aioA genes was the lowest among the four tested arsenic functional genes, it was the second important genes for arsenic distribution. Microbial metabolic activity was the main cause of arsenic transformation, and arsenate reduction by microbes was a key driver of arsenic mobilization in landfills. Moreover, arsenate was reduced to arsenite and further methylated to monomethylarsine (MMA) and dimethylarsine (DMA), decreasing the total arsenic content during the landfill process, but also inducing a new risk because of the arsenic effluent will be more easily as the state of arsenite, MMA, and DMA in the liquid phase. Overall, this study provides a picture of arsenic species transformation and insight into key roles involved in arsenic pollution during landfill processes., (Copyright © 2020 Elsevier B.V. All rights reserved.)